heterozygote


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het·er·o·zy·gote

 (hĕt′ə-rō-zī′gōt′)
n.
An organism that has different alleles at a particular gene locus on homologous chromosomes.
American Heritage® Dictionary of the English Language, Fifth Edition. Copyright © 2016 by Houghton Mifflin Harcourt Publishing Company. Published by Houghton Mifflin Harcourt Publishing Company. All rights reserved.

heterozygote

(ˌhɛtərəʊˈzaɪɡəʊt; -ˈzɪɡəʊt)
n
(Biology) an animal or plant that is heterozygous; a hybrid. Compare homozygote
ˌheterozyˈgosis n
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014

het•er•o•zy•gote

(ˌhɛt ər əˈzaɪ goʊt, -ˈzɪg oʊt)

n.
a hybrid containing genes for two unlike forms of a characteristic, and therefore not breeding true to type.
[1900–05]
Random House Kernerman Webster's College Dictionary, © 2010 K Dictionaries Ltd. Copyright 2005, 1997, 1991 by Random House, Inc. All rights reserved.
ThesaurusAntonymsRelated WordsSynonymsLegend:
Noun1.heterozygote - (genetics) an organism having two different alleles of a particular gene and so giving rise to varying offspring
fertilized ovum, zygote - (genetics) the diploid cell resulting from the union of a haploid spermatozoon and ovum (including the organism that develops from that cell)
genetic science, genetics - the branch of biology that studies heredity and variation in organisms
Based on WordNet 3.0, Farlex clipart collection. © 2003-2012 Princeton University, Farlex Inc.
Translations
heterozigot
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References in periodicals archive ?
"Thrombophilia in this group was defined as factor V Leiden (heterozygote) mutation (n = 17), prothrombin G20210A gene (heterozygote) mutation (n = 12), protein C deficiency (n = 9), or protein S deficiency (n = 4)," wrote the authors.
Miscarriages plus APS means higher clot risk
Here, we present a case of antiphospholipid syndrome accompanied by heterozygote methylene tetrahydrofolate reductase gene mutation (MTHFR) mutation and hemophilia B.
Antiphospholipid syndrome with hemophilia B: A case report represented by recurrent thrombosis/ bleeding attacks
In 1991, it was clarified that PSS resulted from a single nucleotide substitution in the gene encoding the skeletal ryanodine receptor 1 (sRyR1), and this finding allowed accurate diagnosis on the basis of three types: normal, heterozygote and homozygote (Fujii et al., 1991).
Skeletal ryanodine receptor 1-heterozygous PSE (pale, soft and exudative) meat contains a higher concentration of myoglobin than genetically normal PSE meat in pigs
Study of 19 heterozygote AC carriers and of 5 cases of double hemoglobinopathy SC.
Estimated prevalence of sickle cell in Northern Haiti
CYP2C19 heterozygote patients who were also heterozygotes for CYP3A4*1B, CYP3A4*2 and CYP3A4*3 demonstrated 100 per cent eradication.
Genetic polymorphism of CYP2C19 & therapeutic response to proton pump inhibitors
For each migration, a previously identified heterozygote was used as a standard to verify the quality of electrophoresis and facilitate allele identification.
Are bioenergetic properties linked with shell fluctuating asymmetry and heterozygosity in Iceland scallop, Chlamys islandica?
Chi-square analysis showed that 12 of the 14 markers fit the expected 1 heterozygote to 1 homozygote ratio in the B[C.sub.1] generation.
Marker-assessed retention of wheat chromatin in wheat (Triticum aestivum) by jointed goatgrass (Aegilops cylindrica) backcross derivatives
Tests for heterozygote deficiencies and allele frequency differences among populations were performed using GENEPOP, version 1.3 (Raymond and Rousset 1995).
DNA heterozygosity and growth rate in the Atlantic cod Gadus morhua (L)
She has used these data to support her genetic model of handedness, and to argue for a balanced polymorphism with a heterozygote advantage (Annett, 1985).
Annett's theory that individuals heterozygous for the right shift gene are intellectually advantaged: theoretical and empirical problems
Furthermore, it appears that patients who are heterozygote C282Y/ H63D and C282Y/S65C are at increased risk of developing hemochromatosis phenotypically.
Presence of hemochromatosis-associated mutations in Hispanic patients with iron overload
A compound heterozygote HbS/ [[beta].sup.0]-thalassemia will produce symptoms that are:
Answers to 2008 FOCUS continuing education questions
Hemoglobin S/hemoglobin City of Hope compound heterozygote with a SubSaharan genetic background and severe bone marrow hypoplasia.
Heterocigoto compuesto para hemoglobina S/hemoglobina City of Hope con trasfondo genetico subsahariano e hipoplasia severa de medula osea

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